Shame on those malicious, backstabbing women on RHoBH for accusing her of faking this illness.That was a terrible low point for the show, and it's a wonderful thing to see Hadid find worthy platforms where she can share her experience in a way that can shed light to others- and potentially help someone out there also experiencing this debilitating disease.
Yolanda is my heroine warrior! Love to her and great thanks for sharing her journey. Those housewives revealed so much about themselves with their reactions to her struggle. She is so far above those who could not support her. A genuine diamond of a role model.
Out of all the housewives she does the most hands on work/juggling and will actually cook and clean and plan parties and do everything with minimal help. Kyle Richards and Lisa Vanderpump are ones that micro manage staff. Same with Heather Dubrow. As a nurses assistant- I have the most respect out of all the housewives spinoffs for Yolanda. She is 100% class and people who think she's faking it are trash or just plain stupid and ignorant.
Miss Faba I would not call anyone trash. So, uncalled, we are all humans, to call another trash, it to call yourself the same thing.....you are a nurses assistant...quit calling names and become a RN-CNP...we have faith in you!!
I am very thankful for her putting Lyme in the spotlight. Lyme and it's co-infections is such a complicated and difficult illness to diagnose. ( especially if you were not properly diagnosed or treated for years). Proper Treatment feels like torture. It can make every part of your body hurt to the point that you want to take your own life.
Yolanda is not imagining her illness. I have M. E and a condition known as FND with which I get the same symptoms. For Lyme you would have to be bitten by a tick. You often get an obvious bullseye rash. Blood tests can give false positives and negatives. It seems weird that Bella and her son have it as well but they were around horses alot. It's a difficult diagnoses. Either way anyone that says shes neurotic has no idea what these types of illnesses do to peoples lives. Good on her for speaking out. In America people tend to say M.E is Lyme disease. At the end of the way they are both awful illnesss with no cure.
@@wildflowerhoneybee4423 Thanks for your opinion but I refuse to use chronic fatigue as its a piss take and just sounds like people are tired all the time, not the other horrendous symptoms. I have FND Functional Neurologic Disorder but was diagnosed with CFS before.. It just makes me mad. If you tell your boss you've got chronic fatigue syndrome they say everyone's tired. I agree M.E isn't a correct name but calling it chronic tiredness is wrong. I'm with you
so far and few between its barely noticeable!!! the dead beat ones stands out the most coz its the MAJORITY!!! so sorry ...but the stats speaks for itself!!!...do your research!
I know so much about IV PICC line and wound vacc....I went through hell after my 3rd neck surgery. I developed Mersa (MRSA) and had Sepsis. I had to have a fourth neck surgery where my surgeon removed a substantial amount of infected tissue as well as cleaning the rods, plates, screws (etc) in my neck. I was then quarantined to my room at the hospital for quite some time. When I finally got to come home they put an IV PICC line in my arm that stayed there at least 6 months for all the antibiotics that I had to have. Also, a wound vacc was attached to the back of my neck where the surgeon had cut out infected flesh clear down to my cervical spine. The wound vacc was literally used to extract infection from my neck into a machine. A nurse came into my home every other day to change the bandaging from my neck wound and put new bandaging and re-attached the machine to my cervical spine and adjust the IV Picc line. On the days the nurse didn't come into my home, I had to go to see the infectious disease doc and my neck surgeon. It took 6 months of the IV PICC line and 6 months of the wound vacc before I could get those things out of my body and off my neck. But, it took at least 3.5 years before the Mersa and Sepsis was gone. It was a nightmare and I didn't have the luxury of having people help me with house work and such. It was so hard on me mentally and physically. There are things that I just don't remember due to me being so sick. Truly, it was the hardest thing I've ever been through. I'm so thankful it's over with!
She's so brave to put it all out there. I don't even watch the housewives show, I'm listening to her book. And she says everything we are going through so well. We couldn't have a better advocate. ❤
I get that she has been really sick but she doesn't juggle any more on a daily basis than any of the rest of us without housekeepers, personal trainers, cleaners, gardeners etc. I wish her well but I hate when celebrities protest that they juggle too many things when in reality they just micro manage staff.
1000% agree. Lyme disease is actually really manageable. My auntie has it and when she was really ill with it she still juggled kids, her job (mechanic) and she doesn't have the luxury like yolanda does. I'm not saying Lyme disease isn't a horrible disease but it's manageable and the woman has literally been in the media regarding her disease or regarding her children. I dunno sometimes I think she milks it. As my auntie goes to a group that speaks about Lyme disease a lady brought yolanda up and everybody laughed and said the treatment that yolanda recieves she shouldn't be in as much pain as she claims.
Rachael Ferguson I'm glad your aunt is still able to function, but every patient is different. Lyme disease is not a "really manageable disease". I have Lyme disease myself and at my worst I was laying in a dark room, not being able to walk, talk, sit in a wheelchair, eat/drink (I got a feeding tube) or watch TV. Doctors thought I was dying, but thank God I'm still alive today and doing better because of the treatment I received. Unfortunately my case is not rare. It's a horrible disease that effects every patient differently. That's the reason Lyme disease is so hard to treat. If you read Yolanda's book, maybe you will understand what she went through.
I hate it when people compares someone elses situation with another persons situation. ok..your auntie had it , maybe she caught it at an early stage and therefore got treatment early and therefore her situation was not as bad as Yolandas!!!...just one example as to why NOT to compare one persons situation with another!!! was your auntie a celebrity with a million things to be aware and in charge of daily, no matter how much help she has, bottomline is she is still the responsible one should anything go wrong in her daily life in terms of her celebritism, esp!!! so please DONT COMPARE...coz you don't no the real struggles that she had, you only no wat was said of this video...but you don't know the rest of what her OTHER struggles were while dealing with this awful disease!!! shes also been thru a divorce around the same time!!!! and if you never been thru a divorce yourself, PLEASE DONT JUDGE!!!
I agree. I feel like she's thinking that she's something special because she has "Lyymezzz" disease. Many people have it and aren't a drama queen about it like she is. She just seems like an attention whore.
I am just thinking why does she calls herself 'Hadid' as she is already divorced from this man? Not even 'Foster' so why isn't she using her own name? To Dutch? Don't get me wrong I loved her on RHOB.
some women keeps their marital last name, celebrity or not, its that simple!!! why is that an issue? that has nothing to do with Lyme disease, now does it?
*Because some women like to have the same last name as their children!! Plus she was with Mr. Mohamed Hadid the longest.. She had no kids with Mr. David Foster!!*
I have lyme and I didn't ever noticed a bullseye rash.All symptoms came sundely after a mysterious flue like illness.Now it's in my brain and I am suffering debilitating symptoms.But what if you don't have doctor to treat you.In some countries doctors have no idea about lyme.
Yolanda should look up urine therapy to treat and cure Lyme disease completely and she would also find a FREE (affordable) cure for everyone, which is what she says would be the legacy she wants to leave in the world...
Libby Gleeson so does Kris Kristofferson...his medical physicians say dementia...his Naturopath says Chronic Lyme...I'm going with with physicians who went to med school..you?
I adore Yolanda, she is so chic and cool. But, it was amazing she got better after her divorce....could it have been she was depressed and wasn't happy in the marriage, those two things can mimic anything and everything. I believe there is Lyme. But, if a blood test does not show Lyme, it's biologically unreasonable to believe one is ill with lyme. It's a very in vogue disease in which to hide. But, I have great empathy for those suffering.
This is the sort of comment a psychologist would say. Lose the husband now you are all better. Its comments like this that makes people think it's all in your head. I agree about the mind and body connection but you can have remission with these illnesses
Poor Yolanda. It must've been hard to know whether to lie around sniffling in a dressing gown or go out kayaking, to post teary instagrams having yet another utterly pointless treatment, or go out partying all night in some European nightclub.
Evidently, you have know idea what it's like having an autoimmune disease and how it feels to be so very sick. I've been sick for 30+ years, with very brutal symptoms that my doctors take them very seriously. I'd love to defend your point of view, but it is people like you who make the struggle harder. We need more dedicated research and understanding. I don't have Lyme, but my immune system has attract my nervous system and now parts of my body are useless, painful. Some of my tissue has had to be removed or repaired surgically, in long operations. This must be discussed and information and education passed along to help those not as fortunate as yourself... you do know you are fortunate to be well, right? I pray you continue to stay that way. So, please put your nasty, heartless judgments aside and remember you are a member of the human race and can be hurt and damaged by all the conditions that the flesh can be afflicted by....
Deborah Mullan/ A Creative Living Professional I’m the exact same I have a really bad immune system and it’s hard for people to understand the pain u feel everyday. I’ve had loads of medical issues and wen I’m really unwell it’s can sometimes take months for me to feel better and people just don’t understand that u can’t eat properly u can’t sleep ur in pain u sometimes can’t keep ur concentration and it gives me a lot of stress. It’s not nice lol
Odd, Breast implant disease has similar symptoms of Lyme. She seemed to improve immediately after they were removed.
D Jack, I thought so too! One of her implants had ruptured and was attached to her inner chest bones etc. I think that's what made her sick.
Great point. Breast implant Illness is very real.
Bull shit!!!!!
Her Lyme was diagnosed in 2012
Shame on those malicious, backstabbing women on RHoBH for accusing her of faking this illness.That was a terrible low point for the show, and it's a wonderful thing to see Hadid find worthy platforms where she can share her experience in a way that can shed light to others- and potentially help someone out there also experiencing this debilitating disease.
Yolanda is my heroine warrior! Love to her and great thanks for sharing her journey. Those housewives revealed so much about themselves with their reactions to her struggle. She is so far above those who could not support her. A genuine diamond of a role model.
Out of all the housewives she does the most hands on work/juggling and will actually cook and clean and plan parties and do everything with minimal help. Kyle Richards and Lisa Vanderpump are ones that micro manage staff. Same with Heather Dubrow. As a nurses assistant- I have the most respect out of all the housewives spinoffs for Yolanda. She is 100% class and people who think she's faking it are trash or just plain stupid and ignorant.
well said!!! feel the same way!!!
I agree
Miss Faba I would not call anyone trash. So, uncalled, we are all humans, to call another trash, it to call yourself the same thing.....you are a nurses assistant...quit calling names and become a RN-CNP...we have faith in you!!
I am very thankful for her putting Lyme in the spotlight. Lyme and it's co-infections is such a complicated and difficult illness to diagnose. ( especially if you were not properly diagnosed or treated for years). Proper Treatment feels like torture. It can make every part of your body hurt to the point that you want to take your own life.
Linda Southern that's how people feel with cancer, chemo...only they lose their hair and sometimes their lives.
Yolanda is not imagining her illness. I have M. E and a condition known as FND with which I get the same symptoms. For Lyme you would have to be bitten by a tick. You often get an obvious bullseye rash. Blood tests can give false positives and negatives. It seems weird that Bella and her son have it as well but they were around horses alot. It's a difficult diagnoses. Either way anyone that says shes neurotic has no idea what these types of illnesses do to peoples lives. Good on her for speaking out. In America people tend to say M.E is Lyme disease. At the end of the way they are both awful illnesss with no cure.
Jacky Eastwood so, you have chronic fatigue syndrome....just say it...many don't know what M.E. is...the more dramatic name. I know. I'm there. xx
@@wildflowerhoneybee4423
Thanks for your opinion but I refuse to use chronic fatigue as its a piss take and just sounds like people are tired all the time, not the other horrendous symptoms. I have FND Functional Neurologic Disorder but was diagnosed with CFS before.. It just makes me mad. If you tell your boss you've got chronic fatigue syndrome they say everyone's tired. I agree M.E isn't a correct name but calling it chronic tiredness is wrong. I'm with you
M.E and FND are both label diagnosis (mere names), you need to address what causes these symptoms... mostly tickborne infections.
Her sneaky and weird husband didn't hang around long when his wife got sick.
We arent all bad
so far and few between its barely noticeable!!!
the dead beat ones stands out the most coz its the MAJORITY!!!
so sorry ...but the stats speaks for itself!!!...do your research!
Stafford Stafford I think he was her disease. She got better, when he left.
I know so much about IV PICC line and wound vacc....I went through hell after my 3rd neck surgery. I developed Mersa (MRSA) and had Sepsis. I had to have a fourth neck surgery where my surgeon removed a substantial amount of infected tissue as well as cleaning the rods, plates, screws (etc) in my neck. I was then quarantined to my room at the hospital for quite some time. When I finally got to come home they put an IV PICC line in my arm that stayed there at least 6 months for all the antibiotics that I had to have. Also, a wound vacc was attached to the back of my neck where the surgeon had cut out infected flesh clear down to my cervical spine. The wound vacc was literally used to extract infection from my neck into a machine. A nurse came into my home every other day to change the bandaging from my neck wound and put new bandaging and re-attached the machine to my cervical spine and adjust the IV Picc line. On the days the nurse didn't come into my home, I had to go to see the infectious disease doc and my neck surgeon. It took 6 months of the IV PICC line and 6 months of the wound vacc before I could get those things out of my body and off my neck. But, it took at least 3.5 years before the Mersa and Sepsis was gone. It was a nightmare and I didn't have the luxury of having people help me with house work and such. It was so hard on me mentally and physically. There are things that I just don't remember due to me being so sick. Truly, it was the hardest thing I've ever been through. I'm so thankful it's over with!
She's so brave to put it all out there. I don't even watch the housewives show, I'm listening to her book. And she says everything we are going through so well. We couldn't have a better advocate. ❤
i seriously seriously love Yolanda
I get that she has been really sick but she doesn't juggle any more on a daily basis than any of the rest of us without housekeepers, personal trainers, cleaners, gardeners etc. I wish her well but I hate when celebrities protest that they juggle too many things when in reality they just micro manage staff.
Schemvie Schmeves .... Well said 👍👏
1000% agree. Lyme disease is actually really manageable. My auntie has it and when she was really ill with it she still juggled kids, her job (mechanic) and she doesn't have the luxury like yolanda does. I'm not saying Lyme disease isn't a horrible disease but it's manageable and the woman has literally been in the media regarding her disease or regarding her children. I dunno sometimes I think she milks it. As my auntie goes to a group that speaks about Lyme disease a lady brought yolanda up and everybody laughed and said the treatment that yolanda recieves she shouldn't be in as much pain as she claims.
Rachael Ferguson I'm glad your aunt is still able to function, but every patient is different. Lyme disease is not a "really manageable disease". I have Lyme disease myself and at my worst I was laying in a dark room, not being able to walk, talk, sit in a wheelchair, eat/drink (I got a feeding tube) or watch TV. Doctors thought I was dying, but thank God I'm still alive today and doing better because of the treatment I received. Unfortunately my case is not rare. It's a horrible disease that effects every patient differently. That's the reason Lyme disease is so hard to treat. If you read Yolanda's book, maybe you will understand what she went through.
I hate it when people compares someone elses situation with another persons situation. ok..your auntie had it , maybe she caught it at an early stage and therefore got treatment early and therefore her situation was not as bad as Yolandas!!!...just one example as to why NOT to compare one persons situation with another!!! was your auntie a celebrity with a million things to be aware and in charge of daily, no matter how much help she has, bottomline is she is still the responsible one should anything go wrong in her daily life in terms of her celebritism, esp!!! so please DONT COMPARE...coz you don't no the real struggles that she had, you only no wat was said of this video...but you don't know the rest of what her OTHER struggles were while dealing with this awful disease!!! shes also been thru a divorce around the same time!!!! and if you never been thru a divorce yourself, PLEASE DONT JUDGE!!!
I agree. I feel like she's thinking that she's something special because she has "Lyymezzz" disease. Many people have it and aren't a drama queen about it like she is. She just seems like an attention whore.
we suffer in sience, thank you for speaking up for us all.
I am just thinking why does she calls herself 'Hadid' as she is already divorced from this man? Not even 'Foster' so why isn't she using her own name? To Dutch? Don't get me wrong I loved her on RHOB.
some women keeps their marital last name, celebrity or not, its that simple!!!
why is that an issue? that has nothing to do with Lyme disease, now does it?
Janey Bakarbessy Ikr Its kinda weird but kris jenner is also one of them
she wants to have the same last name as her children
*Because some women like to have the same last name as their children!! Plus she was with Mr. Mohamed Hadid the longest.. She had no kids with Mr. David Foster!!*
cos of her children
I have lyme, late version with ACA skinrash on left feed.
You get Lymes in South Africa too now!! Lymes is hell on earth!!!
Very interesting. Lyme disease without the bullseye rash.
I'm pretty sure she has depression
Only 50% gets a bullseye rash.
Not everyone gets it
Also congenital
I have lyme and I didn't ever noticed a bullseye rash.All symptoms came sundely after a mysterious flue like illness.Now it's in my brain and I am suffering debilitating symptoms.But what if you don't have doctor to treat you.In some countries doctors have no idea about lyme.
Yolanda should look up urine therapy to treat and cure Lyme disease completely and she would also find a FREE (affordable) cure for everyone, which is what she says would be the legacy she wants to leave in the world...
Happy birthday Yolanda
Shania Twain has Lyme too
Libby Gleeson so does Kris Kristofferson...his medical physicians say dementia...his Naturopath says Chronic Lyme...I'm going with with physicians who went to med school..you?
She doesn’t need RHOBH #icon
I adore Yolanda, she is so chic and cool. But, it was amazing she got better after her divorce....could it have been she was depressed and wasn't happy in the marriage, those two things can mimic anything and everything. I believe there is Lyme. But, if a blood test does not show Lyme, it's biologically unreasonable to believe one is ill with lyme. It's a very in vogue disease in which to hide. But, I have great empathy for those suffering.
This is the sort of comment a psychologist would say. Lose the husband now you are all better. Its comments like this that makes people think it's all in your head. I agree about the mind and body connection but you can have remission with these illnesses
She looks great .helps been very rich.
So gorgeous God love you
caused by ticks in the great outdoors
mason lane not all ticks have it.
Pinterest chicken with orange & soysauce ginger
This can be caused by implants and botox?
Poor Yolanda. It must've been hard to know whether to lie around sniffling in a dressing gown or go out kayaking, to post teary instagrams having yet another utterly pointless treatment, or go out partying all night in some European nightclub.
It,s all between the ears😆
oh blah... I am sick of this woman talking about this...
I think it is funny that you think I actually go and find this stuff... RUclips has a way of sliding things in from time to time..
Evidently, you have know idea what it's like having an autoimmune disease and how it feels to be so very sick. I've been sick for 30+ years, with very brutal symptoms that my doctors take them very seriously. I'd love to defend your point of view, but it is people like you who make the struggle harder. We need more dedicated research and understanding. I don't have Lyme, but my immune system has attract my nervous system and now parts of my body are useless, painful. Some of my tissue has had to be removed or repaired surgically, in long operations. This must be discussed and information and education passed along to help those not as fortunate as yourself... you do know you are fortunate to be well, right? I pray you continue to stay that way. So, please put your nasty, heartless judgments aside and remember you are a member of the human race and can be hurt and damaged by all the conditions that the flesh can be afflicted by....
Deborah Mullan/ A Creative Living Professional I’m the exact same I have a really bad immune system and it’s hard for people to understand the pain u feel everyday. I’ve had loads of medical issues and wen I’m really unwell it’s can sometimes take months for me to feel better and people just don’t understand that u can’t eat properly u can’t sleep ur in pain u sometimes can’t keep ur concentration and it gives me a lot of stress. It’s not nice lol
she has mental problems i think.
she has Lyme disease...that's not a MENTAL problem!!!
she has both...lol
fun one, for sure on the mental thing !! Hot damn I think we have the answer!!
Lyme can affect your brain, it’s called neuroborreliosis
Attention attention attention control control control what a diva!
Neena M, now she's going the RUclips route trying to make money!
oh here we go
She's so ohhh poor me all the time Jesus ok be sick and don't tell the world let's see if u can do that
Ugh. We get it Yolanda. Old news.
Don’t watch then